EP0827437B2 - Nickel-chronium-based brazing alloys - Google Patents
Nickel-chronium-based brazing alloys Download PDFInfo
- Publication number
- EP0827437B2 EP0827437B2 EP96914570A EP96914570A EP0827437B2 EP 0827437 B2 EP0827437 B2 EP 0827437B2 EP 96914570 A EP96914570 A EP 96914570A EP 96914570 A EP96914570 A EP 96914570A EP 0827437 B2 EP0827437 B2 EP 0827437B2
- Authority
- EP
- European Patent Office
- Prior art keywords
- brazing
- atom percent
- temperature
- brazed
- recited
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 238000005219 brazing Methods 0.000 title claims description 62
- 229910045601 alloy Inorganic materials 0.000 title claims description 52
- 239000000956 alloy Substances 0.000 title claims description 52
- 229910052751 metal Inorganic materials 0.000 claims description 33
- 239000002184 metal Substances 0.000 claims description 33
- 239000000945 filler Substances 0.000 claims description 29
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 claims description 27
- 229910052796 boron Inorganic materials 0.000 claims description 27
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims description 22
- 239000010953 base metal Substances 0.000 claims description 22
- 238000000034 method Methods 0.000 claims description 21
- 229910052710 silicon Inorganic materials 0.000 claims description 20
- 239000010703 silicon Substances 0.000 claims description 20
- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Substances [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 18
- 239000000203 mixture Substances 0.000 claims description 18
- 239000011651 chromium Substances 0.000 claims description 16
- 239000011888 foil Substances 0.000 claims description 16
- 230000008569 process Effects 0.000 claims description 14
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 claims description 13
- 229910052804 chromium Inorganic materials 0.000 claims description 13
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 claims description 11
- 229910052750 molybdenum Inorganic materials 0.000 claims description 11
- 239000011733 molybdenum Substances 0.000 claims description 11
- 229910052759 nickel Inorganic materials 0.000 claims description 11
- 239000000155 melt Substances 0.000 claims description 9
- 229910052742 iron Inorganic materials 0.000 claims description 8
- 238000001816 cooling Methods 0.000 claims description 7
- 239000012535 impurity Substances 0.000 claims description 6
- 238000010791 quenching Methods 0.000 claims description 6
- 230000000171 quenching effect Effects 0.000 claims description 6
- 238000000137 annealing Methods 0.000 claims description 4
- 238000010438 heat treatment Methods 0.000 claims description 3
- 229910052723 transition metal Inorganic materials 0.000 claims description 2
- 150000003624 transition metals Chemical class 0.000 claims description 2
- 238000002425 crystallisation Methods 0.000 claims 1
- 230000008025 crystallization Effects 0.000 claims 1
- 229910021332 silicide Inorganic materials 0.000 claims 1
- 125000004429 atom Chemical group 0.000 description 21
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 18
- 230000007797 corrosion Effects 0.000 description 13
- 238000005260 corrosion Methods 0.000 description 13
- 239000012071 phase Substances 0.000 description 12
- 229910018487 Ni—Cr Inorganic materials 0.000 description 11
- VNNRSPGTAMTISX-UHFFFAOYSA-N chromium nickel Chemical compound [Cr].[Ni] VNNRSPGTAMTISX-UHFFFAOYSA-N 0.000 description 10
- 239000000463 material Substances 0.000 description 9
- 230000008018 melting Effects 0.000 description 9
- 238000002844 melting Methods 0.000 description 9
- 150000002739 metals Chemical class 0.000 description 9
- 239000010935 stainless steel Substances 0.000 description 7
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 6
- 229910001220 stainless steel Inorganic materials 0.000 description 6
- 230000015572 biosynthetic process Effects 0.000 description 5
- 238000007712 rapid solidification Methods 0.000 description 5
- 229910000601 superalloy Inorganic materials 0.000 description 5
- 229910000619 316 stainless steel Inorganic materials 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- 229910021529 ammonia Inorganic materials 0.000 description 3
- 230000003628 erosive effect Effects 0.000 description 3
- 229910001256 stainless steel alloy Inorganic materials 0.000 description 3
- 230000035882 stress Effects 0.000 description 3
- 238000009864 tensile test Methods 0.000 description 3
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 2
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 2
- 229910052802 copper Inorganic materials 0.000 description 2
- 239000010949 copper Substances 0.000 description 2
- 238000004455 differential thermal analysis Methods 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 230000006872 improvement Effects 0.000 description 2
- 238000005304 joining Methods 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 229910052752 metalloid Inorganic materials 0.000 description 2
- 150000002738 metalloids Chemical class 0.000 description 2
- 230000009972 noncorrosive effect Effects 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 239000013535 sea water Substances 0.000 description 2
- 239000006104 solid solution Substances 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 229910000521 B alloy Inorganic materials 0.000 description 1
- 238000002441 X-ray diffraction Methods 0.000 description 1
- CFOAUMXQOCBWNJ-UHFFFAOYSA-N [B].[Si] Chemical compound [B].[Si] CFOAUMXQOCBWNJ-UHFFFAOYSA-N 0.000 description 1
- MRVGWCZKSIQZPS-UHFFFAOYSA-N [Cr].[Ni].[Si].[B] Chemical group [Cr].[Ni].[Si].[B] MRVGWCZKSIQZPS-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 229910052786 argon Inorganic materials 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 238000005266 casting Methods 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 239000002826 coolant Substances 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 238000000151 deposition Methods 0.000 description 1
- 230000001627 detrimental effect Effects 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000000374 eutectic mixture Substances 0.000 description 1
- 238000009689 gas atomisation Methods 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
- -1 halogen salts Chemical class 0.000 description 1
- 229910052809 inorganic oxide Inorganic materials 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 229910000765 intermetallic Inorganic materials 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000001000 micrograph Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 239000000075 oxide glass Substances 0.000 description 1
- 230000001706 oxygenating effect Effects 0.000 description 1
- 229910052763 palladium Inorganic materials 0.000 description 1
- 230000003389 potentiating effect Effects 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 238000010298 pulverizing process Methods 0.000 description 1
- 239000012925 reference material Substances 0.000 description 1
- 239000003507 refrigerant Substances 0.000 description 1
- 238000001878 scanning electron micrograph Methods 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 239000007790 solid phase Substances 0.000 description 1
- 125000006850 spacer group Chemical group 0.000 description 1
- 230000008646 thermal stress Effects 0.000 description 1
- 238000001757 thermogravimetry curve Methods 0.000 description 1
- 230000007704 transition Effects 0.000 description 1
- 238000009692 water atomization Methods 0.000 description 1
Images
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B23—MACHINE TOOLS; METAL-WORKING NOT OTHERWISE PROVIDED FOR
- B23K—SOLDERING OR UNSOLDERING; WELDING; CLADDING OR PLATING BY SOLDERING OR WELDING; CUTTING BY APPLYING HEAT LOCALLY, e.g. FLAME CUTTING; WORKING BY LASER BEAM
- B23K35/00—Rods, electrodes, materials, or media, for use in soldering, welding, or cutting
- B23K35/22—Rods, electrodes, materials, or media, for use in soldering, welding, or cutting characterised by the composition or nature of the material
- B23K35/24—Selection of soldering or welding materials proper
- B23K35/30—Selection of soldering or welding materials proper with the principal constituent melting at less than 1550 degrees C
- B23K35/3033—Ni as the principal constituent
- B23K35/304—Ni as the principal constituent with Cr as the next major constituent
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B23—MACHINE TOOLS; METAL-WORKING NOT OTHERWISE PROVIDED FOR
- B23K—SOLDERING OR UNSOLDERING; WELDING; CLADDING OR PLATING BY SOLDERING OR WELDING; CUTTING BY APPLYING HEAT LOCALLY, e.g. FLAME CUTTING; WORKING BY LASER BEAM
- B23K35/00—Rods, electrodes, materials, or media, for use in soldering, welding, or cutting
- B23K35/02—Rods, electrodes, materials, or media, for use in soldering, welding, or cutting characterised by mechanical features, e.g. shape
- B23K35/0222—Rods, electrodes, materials, or media, for use in soldering, welding, or cutting characterised by mechanical features, e.g. shape for use in soldering, brazing
- B23K35/0233—Sheets, foils
Definitions
- This invention relates to brazing filler metals composed of nickel-chromium-based alloys containing transition metals such as iron and molybdenum and certain metalloids; and more particularly to multicomponent alloys containing nickel, chromium, iron, molybdenum, boron, and silicon, which are particularly useful for brazing metals at high temperatures to produce high strength and corrosion-resistant brazements
- Brazing is a process for joining metal parts, often of dissimilar composition, to each other.
- a brazing filler metal that has a melting point lower than that of the parts to be joined is interposed between the parts to form an assembly.
- the assembly is then heated to a temperature sufficient to melt the brazing filler metal.
- a strong, preferably corrosion resistant, joint is formed.
- plate-type heat exchangers One class of products produced by brazing processes is plate-type heat exchangers.
- the plate-and-frame heat exchangers have been widely used in food, chemical, aerospace and other process industries.
- a standard plate-and-frame heat exchanger consists of a number of alternating corrugated/flat metal sheets kept in tight, sealed contact with each other using gaskets or being brazed.
- brazed heat exchangers are stronger and more suitable for high temperature/high pressure applications than those with the gasket-type of sealing.
- These plates are mounted on a frame that may be free-standing or are built into a supporting structure. An elaborate system of channels is formed by these plates in which two, one hot and one cool, liquid and/or gas media flow separately exchanging heat and thus saving energy.
- heat exchanger brazes should be free from any brittle phases in order to provide high ductility and strength combined with high corrosion resistance.
- Nickel-chromium-based filler metals containing boron and silicon when crystallizing from the liquid state, form the eutectic mixture of solid solution and intermetallic solid phases. It is well known that the presence of intermetallic phases rich in boron and silicon results in formation of brazes which are brittle, poorly resistant to fatigue, and susceptible to corrosion. Conventional brazing is typically carried out with a holding time at brazing temperature of about 15-30 min. Such holding time is insufficient to deplete the braze of silicon and boron by dissolving these components into adjoining base metal parts of sufficient thickness to a degree that the intermetallic phases cannot be formed.
- Brazing filler metals consisting of nickel-chromium-based alloys have been developed which exhibit high temperature strength and good corrosion resistance. Such alloys have been disclosed, for example, in US Pat. Nos. 4,302,515, 4,745,037, and 4,543,135. The alloys disclosed in these patents, however, each exhibit drawbacks which make them unsuitable for brazing products which require prolonged service life in highly corrosive environments or having a sufficient thickness to provide sufficient braze cross-section with high effective joint strength. For example, the alloys disclosed in US Pat. Nos. 4,302,515 and 4,745,037 contain boron in substantial amount(s) (at least 9 to 18 atom percent).
- boron diffuses extensively out of the joint area into to stainless steel and superalloy base metals when subjected to brazing at very high temperatures and forms intermetallic boride phases detrimental to base metal mechanical fatigue and corrosion resistance.
- boron with its small atomic radius, diffuses along grain boundaries forming therein intermetallic borides and resulting in brittle fracture under loading at elevated temperatures. Therefore, alloys containing a large amount of boron are not suitable for brazing products designed to withstand high temperature, high stress and high fatigue environments, i.e., for example, stainless steel and/or superalloy honeycomb structures employed in airfoils and plate-type heat exchangers subjected to variable high pressure/high temperature conditions. Moreover, this is of the critical importance for structures in which the thin gage (about 0.1-0.05 mm thick) base metal components are used.
- the present invention provides an improved brazing filler metal which possesses high temperature melting characteristics and low erosion of base metal parts. Brazements produced using such filler metal have substantially uniform microstructure and possess high strength at elevated temperatures. In addition, the brazements exhibit high corrosion resistance in various corrosive environments.
- Brazing alloys particularly suited for use as the filler metal consist of nickel-chromium-based alloys having a composition defined by the following formula: Cr a Fe b Si c B d Mo e Ni balance , where the subscripts "a”, “b”, “c”, “d”, and “e” are in atomic percent, "a” ranges from 9.5 to 16.5, “b” ranges from 0 to about 5, “c” ranges from 10 to 15, “d” ranges from 6 to 7, “e” ranges from 0 to 5 and the balance is nickel plus incidental impurities.
- the invention provides brazing filler metals in the form of homogeneous ductile foils which are composed of metastable materials preferably having at least 80% amorphous structure.
- an improved process for joining stainless steels and/or superalloys honeycomb structures and plate heat exchangers, which process comprising the steps of:
- the invention further relates to a brazed article produced by the above process.
- the brazing material In any brazing process, the brazing material must have a melting point that will be sufficiently high to provide strength to meet service requirements of the metal parts to be brazed together. Further, the material must be compatible, both chemically and metallurgically, with the base metal parts being brazed. Also, the brazing material must be more noble than the base metal being brazed to avoid corrosion. Ideally, the brazing material should be in 100% metal containing foil form so that complex shapes may be stamped therefrom and so that brazing of complex structures can be readily accomplished.
- brazing foils should be homogeneous and ductile; that is, contain no binders or other materials that would otherwise form voids or contaminating residues during brazing, and exhibit sufficient flexibility such that the foil can be bent to a round radius as small as about 10 times the foil thickness without fracture.
- brazing conditions should be sufficient for formation of a strong and ductile braze microstructure that is substantially free from brittle silicon/boron containing intermetallic phases.
- multicomponent nickel-chromium-based alloys which exhibit a liquidus of at least about 1090 degree(s) C, and are particularly suitable for brazing stainless steel and superalloys.
- the brazing filler metals have a composition consisting of 0 to 5 atom percent iron, 9.5 to 16.5 atom percent chromium, 10 to 15 atom percent silicon, 6 to 7 atom percent boron, 0 to 5 atom percent molybdenum, the balance being essentially nickel and incidental impurities.
- Each constituent imparts certain of the unique combination of characteristics attributed to the Ni-Cr-based alloys of the present invention.
- the relatively high liquidus of the alloys of the present invention results principally from the high nickel-chromium and moderate silicon-boron content in the alloys.
- brazements produced with filler metal composed of these alloys can withstand high temperature service conditions.
- chromium concentration of the filler metal is higher than 10 wt.%, a well known threshold value above which corrosion resistant, chromium-containing alloys develop a passive, protective film.
- the amount of chromium present in the alloy ranges from 9.5 to 16.5 atom percent, and preferably from about 12 to about 15 atom percent. Iron, when present in the amount of 0 to 5, and preferably about 1 to about 4 atom percent, improves compatibility of the filler metal with the base metal.
- Boron and silicon are added to enhance the ability of the alloys to exist in the amorphous form and to lower the melting point of the alloys.
- boron is present,in the amount of 6 to 7, and preferably about 6.2 to about 6.8 atom percent, to improve amorphability and interaction between base and filler metals.
- the silicon content ranges from 10 to 15, and preferably from about 11.0 to about 13.5 atom percent. In these amounts silicon operates to induce formation of the amorphous structure and contributes to brazeability of the filler metal.
- the total boron and silicon content cannot be so great as to cause excessive erosion of the base metal during brazing or to cause the excessive formation of a separate phase of brittle intermetallic compounds in the brazement.
- the total boron and silicon content of the filler metal ranges from about 16 to about 22 atom percent, and more preferably ranges from 18 to about 20 atom percent.
- molybdenum is also present in an amount ranging from 0 to 5 atom percent, and more preferably in an amount ranging from about 3.0 to about 3.5 atom percent.
- the role of molybdenum in the alloys of the present invention is to preserve the low melting temperature of the alloy while increasing the overall strength of the passive film forming on brazes. More specifically, molybdenum greatly reduces the incidence of pitting of brazed joints which may be formed using alloys of the present invention.
- nickel in alloys of the present invention greatly improves their resistance to certain non-oxygenating corrosive media. Nickel also imparts other desired properties, such as amorphability, ductility and the like.
- the alloys of the present invention can be produced in various forms, such as powders, foils, ribbons and wires by application of various well known techniques. Methods commonly used to fabricate alloys in powder form include gas or water atomization or mechanical pulverization. The most preferred method used to fabricate alloys of the present invention into foils, ribbons or wire is rapid solidification.
- the alloys of the present invention exhibit a number of advantageous properties neither recognized nor disclosed heretofore. These alloys exhibit a high melting temperature, as compared to prior art nickel-chromium-based compositions, because of the low concentration of boron. In addition, the alloys exhibit low erosion of base metal and no significant diffusion problems, generally associated with high boron-containing alloys, because boron concentration is kept at a minimum. At the same time, boron concentration, coupled with sufficient silicon concentration, enables the production of a ductile and thick ribbon product by rapid solidification technology.
- the alloys of the present invention do not substantially erode the base metal, thereby preserving the integrity of thin fin parts used in honeycomb and plate-type structures.
- the alloys of the present invention are ordinarily produced in the form of homogeneous, ductile foils or wires by casting alloys of the above described composition using rapid solidification techniques. More specifically, the homogeneous brazing filler metals of the present invention are fabricated by a rapid solidification process which comprises forming a melt of the composition, and quenching the melt on a rotating quenching wheel at a rate of at least about 10 5 degree(s) C per second. Such a process is disclosed in U.S. Pat. No. 4,142,571. Under these quenching conditions, a metastable, homogeneous ductile product is obtained.
- the metastable material may be amorphous, in which case there is no long range order as evidenced by X-ray diffraction patterns which show a diffuse halo, similar to that observed for inorganic oxide glasses.
- the microstructure of alloys of the present invention contained at least 80% of amorphous phase to achieve superior ductility, and most preferably it is at least about 90% amorphous.
- Foils produced by the rapid solidification process described herein are between about 13 and about 100 micrometers thick, ordinarily between about 13 and about 76 micrometers thick and up to 200 mm wide and more. Because these products are homogeneous (i.e., of substantially uniform composition in all directions), brazements produce therefrom are quite uniform and substantially free of voids.
- the alloy has a composition of 9.5 to 16.5 atom percent chromium, 0 to 5 atom percent iron, 10 to 15 atom percent silicon, 6 to 7 atom percent boron, and 0 to 5 atom percent molybdenum, the balance being essentially nickel and incidental impurities.
- the alloys within this most preferred embodiment exhibit a melting temperature range of between about 960 degree(s) C and about 1200 degree(s) C and, most preferably, range from about 1030 degree(s) C to about 1130 degree(s) C.
- the specific advantages of these alloys include the ability to braze at reasonably high temperatures and to provide a brazement which can be employed at elevated temperature under high stress, high corrosive environment and high fatigue conditions without any significant degradation of mechanical properties.
- Alloys produced in accordance with the invention are particularly suited for the brazing of stainless steel honeycomb and plate-type heat exchanger structures used in aircraft industries, power plant, food, chemical and other processing industries.
- the brazing process of the invention provides a marked improvement in joint mechanical strength and corrosion and fatigue resistance. This marked improvement is due to the increased holding time (preferably about 2 or more hours) at a brazing temperature of at least 50°C higher than liquidus.
- Ribbons about 2.54 to about 200 mm (about 0.1 to about 8 inches) wide and about 13 to about 76 micrometers (about 0.0005 to about 0.003 inch) thick are formed by continually depositing a melt of each of the compositions set forth in Table 1 below, by overpressure of argon onto a rapidly rotating copper chill wheel (surface speed about 3000 to about 6000 ft/min). Metastable homogeneous ribbons having substantially glassy structure were produced. The liquidus and solidus temperatures of the ribbons described in Table 1 are determined by the Differential Thermal Analysis (DTA) technique. The individual samples are heated side by side with an inert reference material at a uniform rate, and the temperature difference between them is measured as a function of temperature. A thermogram is produced (a plot of heat-energy change vs. temperature) from which the beginning of melting and the end of melting, known respectively as solidus and liquidus temperatures, are determined. The values are reported in Table 1 below.
- DTA Differential Thermal Analysis
- AISI 316 stainless steel Tensile test specimens are cut from AISI 316 stainless steel, in strip form.
- the composition of AISI 316 stainless steel is given in Table 2.
- AISI 316 Composition, weight % Fe Ni Cr C Mn Si Mo Others Bal 10-14 16-18 0.08 2.0 1.0 2-3 075
- the tensile specimens are dimensioned and fabricated as lap shear specimens per AWS C3.2-63. The specimens are cut perpendicularly to the length direction. The thickness is 0.3175 cm (0.125 inch). Braze joints are of the lap type, with the lap dimensions carefully controlled to 1.27 cm (0.5 inch). Brazing specimens are degreased with benzene. Lap joints containing brazing ribbons of the invention are assembled with the ribbons side by side, the length of the lap joint.
- the ribbons act as spacers. A single spot weld is used to hold the assembly together, as is a common industrial practice.
- a brazing alloy of the invention an amorphous ductile ribbon of nominal composition of sample No. 1 and having dimensions 50 ⁇ m (about 0.002 inch) thick by 12.5 mm (0.5 inch) wide is used to braze these test specimens.
- brazing is done in a vacuum furnace which is evacuated to a pressure of 1.33X10 -2 Pa (10 -4 Torr).
- the brazing conditions are outlined in Table 3.
- the typical microstructure of a joint after such brazing is presented in Fig. 1.
- Intermetallic silicon/boron containing phases are observed only outside of the joint area, namely, in a thick fillet containing an excessive amount of the filler metal.
- the joint itself is uniform and has a strong and ductile single phase structure consisting of a nickel-chromium-based solid solution phase.
Landscapes
- Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Pressure Welding/Diffusion-Bonding (AREA)
- Heat Treatment Of Articles (AREA)
- Laminated Bodies (AREA)
Description
| |||||||
Fe | Ni | Cr | C | Mn | Si | Mo | Others |
Bal | 10-14 | 16-18 | 0.08 | 2.0 | 1.0 | 2-3 | 075 |
Sample | Brazing Conditions | Post Brazing Annealing | Minimum Tensile Strength | |||
Temp., °C | Time, min | Temp., °C | Time, min | MPa | ksi | |
1 | 1155 | 10 | - | - | 43 | 6.23 |
2 | 1155 | 75 | - | - | 180 | 26.1 |
3 | 1165 | 150 | 1100 | 180 | 263 | 38.1 |
4 | 1175 | 150 | 1100 | 180 | 295 | 42.7 |
5 | 1190 | 150 | 1100 | 180 | 360 | 52.2 |
6 | 1190 | 250 | 1100 | 180 | 353 | 51.1 |
7 | 1190 | 250 | 1100 | 60 | 306 | 44.4 |
Claims (10)
- An alloy consisting of a composition defined by the formula:
CraFebSicBdMoeNibalance, the subscripts "a", "b", "c", "d", and "e" being in atomic percent, where "a" ranges from 9.5 to 16.5, "b" ranges from 0 to 5, "c" ranges from 10 to 15, "d" ranges from 6 to 7, and "e" ranges from 0 to 5, the balance being nickel and incidental impurities. - An alloy, as recited by claim 1, which is at least about 80% glassy.
- An alloy, as recited by claim 2, having a solidus of at least about 960 degree(s) C and a liquidus ranging from at least about 1090 degree(s) C to about 1250 degree(s) C.
- A homogeneous, ductile brazing foil formed from the alloy of claim 2.
- A brazing foil, as recited by claim 3 having a thickness ranging from about 20 µm to 90 µm.
- A brazed article produced by a process comprising the steps of:(a) forming a melt of a composition consisting of 0 to 5 atom percent iron, 9.5 to 16.5 atom percent chromium, 10 to 15 atom percent silicon, 6 to 7 atom percent boron, 0 to 5 atom percent molybdenum, the balance being essentially nickel and incidental impurities and quenching the melt on a moving chill surface at a rate of at least about 105°C/sec to produce a homogeneous, ductile brazing foil;(b) interposing said filler metal between base metal parts to form an assembly;(c) heating the assembly to a temperature of about 50°C above the liquidus temperature of said brazing filler metal and holding at said temperature for a time sufficient to dissolve intermetallic brittle phases formed during brazing and afterwards cooling to about 1000°C and holding at said temperature for a time sufficient for postbrazing annealing of said structure;(d) cooling the assembly to provide a brazed structure.
- A brazed article as recited by claim 6, wherein said article has a brazed joint, the strength of which is greater than 200MPa.
- A brazed article as recited by any of claims 6 of 7, said article having a brazement substantially free from brittle intermetallic phases.
- A brazed article as recited by claim 8, wherein said intermetallic phases are predominantly borides and silicides of transition metals which had been initially formed upon crystallization of said filler metal and were thereafter dissolved into said base metal parts during brazing.
- A process for brazing base metal parts comprising the steps of:(a) forming a melt of a composition consisting of 0 to 5 atom percent iron, 9.5 to 16.5 atom percent chromium, 10 to 15 atom percent silicon, 6 to 7 atom percent boron, 0 to 5 atom percent molybdenum, the balance being essentially nickel and incidental impurities and quenching the melt on a moving chill surface at a rate of at least about 105°C/sec to produce a homogeneous, ductile brazing foil;(b) interposing said filler metal between base metal parts to form an assembly;(c) heating the assembly to a temperature of about 50°C above the liquidus temperature of said brazing filler metal and holding at said temperature for a time sufficient to dissolve intermetallic brittle phases formed during brazing and afterwards cooling to about 1000°C and holding at said temperature for a time sufficient for postbrazing annealing of said structure;(d) cooling the assembly to provide a brazed structure.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US44700195A | 1995-05-22 | 1995-05-22 | |
US447001 | 1995-05-22 | ||
PCT/US1996/006195 WO1996037335A1 (en) | 1995-05-22 | 1996-05-02 | Nickel-chronium-based brazing alloys |
Publications (3)
Publication Number | Publication Date |
---|---|
EP0827437A1 EP0827437A1 (en) | 1998-03-11 |
EP0827437B1 EP0827437B1 (en) | 2000-08-23 |
EP0827437B2 true EP0827437B2 (en) | 2005-09-14 |
Family
ID=23774613
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP96914570A Expired - Lifetime EP0827437B2 (en) | 1995-05-22 | 1996-05-02 | Nickel-chronium-based brazing alloys |
Country Status (7)
Country | Link |
---|---|
EP (1) | EP0827437B2 (en) |
JP (1) | JP3940167B2 (en) |
DE (1) | DE69609962T3 (en) |
DK (1) | DK0827437T3 (en) |
IL (1) | IL118089A (en) |
RU (1) | RU2167751C2 (en) |
WO (1) | WO1996037335A1 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US8052809B2 (en) | 2007-06-15 | 2011-11-08 | Vacuumschmelze Gmbh & Co. Kg | Iron-based brazing foil and method for brazing |
Families Citing this family (21)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1997043082A1 (en) * | 1996-05-14 | 1997-11-20 | Alliedsignal Inc. | Nickel-chromium-based brazing alloys |
IT1313883B1 (en) * | 1999-12-17 | 2002-09-24 | Edison Termoelettrica Spa | ARTICLE BASED ON A METAL ALLOY OF NICKEL CHROME AND ELEMENTIMETALLOIDS INCLUDING PRECIPITATED MICROCRYSTALLINE, METAL ALLOY |
SE523855C2 (en) | 2000-11-10 | 2004-05-25 | Alfa Laval Corp Ab | Iron-based brazing material for joining elm and soldered product made herewith |
US6551421B1 (en) * | 2000-11-20 | 2003-04-22 | Honeywell International Inc. | Brazing foil performs and their use in the manufacture of heat exchangers |
SE519062C2 (en) * | 2001-05-03 | 2003-01-07 | Alfa Laval Corp Ab | Ways of soldering thin heat exchanger plates and soldered plate heat exchangers prepared according to the method |
SE524928C2 (en) * | 2001-06-05 | 2004-10-26 | Alfa Laval Corp Ab | Iron-based brazing material for joining elements through brazing and brazed product made herewith |
DE102005039803A1 (en) * | 2005-08-22 | 2007-05-24 | Vacuumschmelze Gmbh & Co. Kg | Brazing foil on iron-nickel base and method for brazing |
DE102006036195A1 (en) * | 2006-08-01 | 2008-02-07 | Vacuumschmelze Gmbh & Co. Kg | Nickel-based brazing alloy and brazing method |
US8894780B2 (en) | 2006-09-13 | 2014-11-25 | Vacuumschmelze Gmbh & Co. Kg | Nickel/iron-based braze and process for brazing |
SE531988C2 (en) * | 2006-11-17 | 2009-09-22 | Alfa Laval Corp Ab | Soldering material and method of soldering with this material |
CA2717344C (en) * | 2008-03-19 | 2019-06-04 | Hoeganaes Ab (Publ) | Iron-chromium based brazing filler metal |
ES2351281B1 (en) * | 2009-02-03 | 2011-09-28 | Valeo Termico, S.A. | HEAT EXCHANGER FOR GASES, ESPECIALLY OF EXHAUST GASES OF AN ENGINE. |
CN102079619B (en) * | 2009-11-27 | 2012-02-15 | 洛阳兰迪玻璃机器股份有限公司 | Glass plate combination sealing method |
DK2644312T3 (en) | 2012-03-28 | 2019-02-25 | Alfa Laval Corp Ab | Hitherto unknown soldering concept |
EP2853332A1 (en) | 2013-09-26 | 2015-04-01 | Alfa Laval Corporate AB | A novel brazing concept |
ES2756850T3 (en) | 2013-09-26 | 2020-04-27 | Alfa Laval Corp Ab | Method of joining metal parts using a melting point depressant layer |
KR20170105117A (en) * | 2015-03-05 | 2017-09-18 | 히타치 긴조쿠 가부시키가이샤 | Alloy brazing powder and joined component |
RU2625924C2 (en) * | 2015-10-13 | 2017-07-19 | Общество с ограниченной ответственностью "МИФИ-АМЕТО" | Process of obtaining quick-resistant boron-free solder nickel brazing products from corrosive-steel, solder, peak connection and method of its obtaining |
DE102019120862A1 (en) | 2019-08-01 | 2021-02-04 | Benteler Automobiltechnik Gmbh | Process for manufacturing a plate heat exchanger and plate heat exchanger |
US20230038008A1 (en) | 2021-07-26 | 2023-02-09 | Vacuumschmelze Gmbh & Co. Kg | Brazing foil, object and method for brazing |
JP7442238B1 (en) * | 2023-06-09 | 2024-03-04 | 東京ブレイズ株式会社 | Brazing filler metals, brazing materials, and methods of manufacturing them |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2714760A (en) * | 1951-07-02 | 1955-08-09 | Curtiss Wright Corp | Method of brazing and joint produced thereby |
US4745037A (en) * | 1976-12-15 | 1988-05-17 | Allied Corporation | Homogeneous, ductile brazing foils |
EP0051461A1 (en) * | 1980-10-30 | 1982-05-12 | Allied Corporation | Homogeneous ductile brazing foils |
US4543135A (en) * | 1982-11-15 | 1985-09-24 | Allied Corporation | Nickel high-chromium base brazing filler metal for high temperature applications |
-
1996
- 1996-04-30 IL IL11808996A patent/IL118089A/en not_active IP Right Cessation
- 1996-05-02 EP EP96914570A patent/EP0827437B2/en not_active Expired - Lifetime
- 1996-05-02 DK DK96914570T patent/DK0827437T3/en active
- 1996-05-02 JP JP53568396A patent/JP3940167B2/en not_active Expired - Fee Related
- 1996-05-02 DE DE69609962T patent/DE69609962T3/en not_active Expired - Lifetime
- 1996-05-02 WO PCT/US1996/006195 patent/WO1996037335A1/en active IP Right Grant
- 1996-05-02 RU RU97120722/02A patent/RU2167751C2/en active
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US8052809B2 (en) | 2007-06-15 | 2011-11-08 | Vacuumschmelze Gmbh & Co. Kg | Iron-based brazing foil and method for brazing |
Also Published As
Publication number | Publication date |
---|---|
EP0827437A1 (en) | 1998-03-11 |
JP3940167B2 (en) | 2007-07-04 |
EP0827437B1 (en) | 2000-08-23 |
DE69609962T3 (en) | 2006-03-16 |
WO1996037335A1 (en) | 1996-11-28 |
DE69609962D1 (en) | 2000-09-28 |
JPH11505178A (en) | 1999-05-18 |
DK0827437T3 (en) | 2000-11-20 |
IL118089A (en) | 2001-06-14 |
DE69609962T2 (en) | 2001-01-04 |
IL118089A0 (en) | 1996-08-04 |
RU2167751C2 (en) | 2001-05-27 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
EP0827437B2 (en) | Nickel-chronium-based brazing alloys | |
US6200690B1 (en) | Nickel-chromium-based brazing alloys | |
EP0014335B1 (en) | Homogeneous ductile brazing foils | |
US4148973A (en) | Homogeneous, ductile brazing foils | |
US4745037A (en) | Homogeneous, ductile brazing foils | |
US4543135A (en) | Nickel high-chromium base brazing filler metal for high temperature applications | |
US4283225A (en) | Process for fabricating homogeneous, ductile brazing foils and products produced thereby | |
US4314661A (en) | Homogeneous, ductile brazing foils | |
EP1082190B1 (en) | Cobalt-chromium-palladium-based brazing alloys | |
EP0020965B1 (en) | Metal articles brazed with a homogeneous, ductile cobalt based brazing material | |
EP0051461A1 (en) | Homogeneous ductile brazing foils | |
US4508257A (en) | Method of brazing with nickel based alloy | |
CA1161284A (en) | Homogeneous, ductile brazing foils | |
US4801072A (en) | Homogeneous, ductile brazing foils | |
US4480016A (en) | Homogeneous, ductile brazing foils | |
EP0056141B1 (en) | Homogeneous ductile nickel-palladium based brazing foils | |
US4448618A (en) | Nickel based brazing filler metals | |
US4316572A (en) | Homogeneous, ductile brazing foils | |
WO1997043082A1 (en) | Nickel-chromium-based brazing alloys | |
US4658537A (en) | Nickel high-chromium base brazing filler metal for high temperature applications | |
US4712603A (en) | Method of making a nickle high-chromium base brazing filler metal | |
WO1989010418A1 (en) | Nickel-palladium-based brazing alloys | |
JPH02151377A (en) | Alloy foil for liquid phase diffusion bonding of Cr-containing materials that can be bonded in an oxidizing atmosphere | |
MXPA00011783A (en) | Cobalt-chromium-palladium-based brazing alloys |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PUAI | Public reference made under article 153(3) epc to a published international application that has entered the european phase |
Free format text: ORIGINAL CODE: 0009012 |
|
17P | Request for examination filed |
Effective date: 19971022 |
|
AK | Designated contracting states |
Kind code of ref document: A1 Designated state(s): DE DK FR GB IT SE |
|
17Q | First examination report despatched |
Effective date: 19980330 |
|
GRAG | Despatch of communication of intention to grant |
Free format text: ORIGINAL CODE: EPIDOS AGRA |
|
GRAG | Despatch of communication of intention to grant |
Free format text: ORIGINAL CODE: EPIDOS AGRA |
|
GRAH | Despatch of communication of intention to grant a patent |
Free format text: ORIGINAL CODE: EPIDOS IGRA |
|
GRAH | Despatch of communication of intention to grant a patent |
Free format text: ORIGINAL CODE: EPIDOS IGRA |
|
RAP1 | Party data changed (applicant data changed or rights of an application transferred) |
Owner name: HONEYWELL INTERNATIONAL INC. |
|
GRAA | (expected) grant |
Free format text: ORIGINAL CODE: 0009210 |
|
AK | Designated contracting states |
Kind code of ref document: B1 Designated state(s): DE DK FR GB IT SE |
|
REF | Corresponds to: |
Ref document number: 69609962 Country of ref document: DE Date of ref document: 20000928 |
|
ET | Fr: translation filed | ||
ITF | It: translation for a ep patent filed | ||
REG | Reference to a national code |
Ref country code: DK Ref legal event code: T3 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: DK Payment date: 20010314 Year of fee payment: 6 |
|
PLBQ | Unpublished change to opponent data |
Free format text: ORIGINAL CODE: EPIDOS OPPO |
|
PLBI | Opposition filed |
Free format text: ORIGINAL CODE: 0009260 |
|
PLBF | Reply of patent proprietor to notice(s) of opposition |
Free format text: ORIGINAL CODE: EPIDOS OBSO |
|
26 | Opposition filed |
Opponent name: VACUUMSCHMELZE GMBH & CO. KG Effective date: 20010502 |
|
PLBF | Reply of patent proprietor to notice(s) of opposition |
Free format text: ORIGINAL CODE: EPIDOS OBSO |
|
PLBF | Reply of patent proprietor to notice(s) of opposition |
Free format text: ORIGINAL CODE: EPIDOS OBSO |
|
REG | Reference to a national code |
Ref country code: GB Ref legal event code: IF02 |
|
PLBF | Reply of patent proprietor to notice(s) of opposition |
Free format text: ORIGINAL CODE: EPIDOS OBSO |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: DK Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20020531 |
|
REG | Reference to a national code |
Ref country code: DK Ref legal event code: EBP |
|
PLAW | Interlocutory decision in opposition |
Free format text: ORIGINAL CODE: EPIDOS IDOP |
|
APAC | Appeal dossier modified |
Free format text: ORIGINAL CODE: EPIDOS NOAPO |
|
APBQ | Date of receipt of statement of grounds of appeal recorded |
Free format text: ORIGINAL CODE: EPIDOSNNOA3O |
|
REG | Reference to a national code |
Ref country code: GB Ref legal event code: 732E |
|
REG | Reference to a national code |
Ref country code: FR Ref legal event code: TP |
|
APAA | Appeal reference recorded |
Free format text: ORIGINAL CODE: EPIDOS REFN |
|
APBU | Appeal procedure closed |
Free format text: ORIGINAL CODE: EPIDOSNNOA9O |
|
PUAH | Patent maintained in amended form |
Free format text: ORIGINAL CODE: 0009272 |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: PATENT MAINTAINED AS AMENDED |
|
RIC2 | Information provided on ipc code assigned after grant |
Ipc: 7C 22C 19/05 B Ipc: 7B 23K 35/14 B Ipc: 7B 23K 35/30 A |
|
27A | Patent maintained in amended form |
Effective date: 20050914 |
|
AK | Designated contracting states |
Kind code of ref document: B2 Designated state(s): DE DK FR GB IT SE |
|
APAH | Appeal reference modified |
Free format text: ORIGINAL CODE: EPIDOSCREFNO |
|
REG | Reference to a national code |
Ref country code: SE Ref legal event code: RPEO |
|
REG | Reference to a national code |
Ref country code: FR Ref legal event code: TP |
|
ET3 | Fr: translation filed ** decision concerning opposition | ||
PLAB | Opposition data, opponent's data or that of the opponent's representative modified |
Free format text: ORIGINAL CODE: 0009299OPPO |
|
REG | Reference to a national code |
Ref country code: FR Ref legal event code: PLFP Year of fee payment: 20 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: SE Payment date: 20150512 Year of fee payment: 20 Ref country code: GB Payment date: 20150429 Year of fee payment: 20 Ref country code: DE Payment date: 20150428 Year of fee payment: 20 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: IT Payment date: 20150515 Year of fee payment: 20 Ref country code: FR Payment date: 20150508 Year of fee payment: 20 |
|
REG | Reference to a national code |
Ref country code: DE Ref legal event code: R071 Ref document number: 69609962 Country of ref document: DE |
|
REG | Reference to a national code |
Ref country code: GB Ref legal event code: PE20 Expiry date: 20160501 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: GB Free format text: LAPSE BECAUSE OF EXPIRATION OF PROTECTION Effective date: 20160501 |